| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:653327-653582 | Common:2; Rare:68 | ||||
| chr20:768487-768695 | Rare:41 | ||||
| chr20:1118424-1118860 | Common:6; Rare:158 | ||||
| chr20:1325270-1325454 | Rare:46 | ||||
| chr20:1392866-1393155 | Common:1; Rare:102 | ||||
| chr20:1894164-1894626 | Common:3; Rare:114 | ||||
| chr20:1895066-1895418 | Common:2; Rare:98 | ||||
| chr20:2102364-2102686 | Common:1; Rare:94 | ||||
| chr20:2470686-2471087 | Common:4; Rare:135 | ||||
| chr20:2652381-2652642 | Common:7; Rare:94 | ||||
| chr20:2655407-2656027 | Common:1; Rare:192 | ||||
| chr20:2656074-2656537 | Common:1; Rare:149; Clinvar (benign):1 | ||||
| chr20:2656539-2656636 | Rare:47 | ||||
| chr20:2659515-2659722 | Rare:79; Clinvar:2 | ||||
| chr20:2664160-2664224 | Rare:34 |